Cas 123076-16-4,methyl O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-(1<*>6)-2,3,4-tri-O-benzoyl-β-D-galactopyranoside

123076-16-4

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Basic information

Product Name: methyl O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-(1<*>6)-2,3,4-tri-O-benzoyl-β-D-galactopyranoside
Synonyms: methyl O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-(1<*>6)-2,3,4-tri-O-benzoyl-β-D-galactopyranoside
CAS NO:123076-16-4
Molecular Formula:
Molecular Weight: 836.801
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: methyl O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-(1<*>6)-2,3,4-tri-O-benzoyl-β-D-galactopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-(1<*>6)-2,3,4-tri-O-benzoyl-β-D-galactopyranoside(123076-16-4)
EPA Substance Registry System: methyl O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-(1<*>6)-2,3,4-tri-O-benzoyl-β-D-galactopyranoside(123076-16-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 123076-16-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 123076-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,0,7 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 123076-16:
(8*1)+(7*2)+(6*3)+(5*0)+(4*7)+(3*6)+(2*1)+(1*6)=94
94 % 10 = 4
So 123076-16-4 is a valid CAS Registry Number.

123076-16-4Upstream product

123076-16-4Downstream Products

123076-16-4Relevant academic research and scientific papers

Versatile synthesis and mechanism of activation of S-benzoxazolyl glycosides

Kamat, Medha N.,Rath, Nigam P.,Demchenko, Alexei V.

, p. 6938 - 6946 (2008/02/11)

(Chemical Equation Presented) As a part of a program for developing new efficient procedures for stereoselective glycosylation, a range of S-benzoxazolyl (SBox) glycosides have been synthesized. The mechanistic aspects of the SBox moiety activation for gl

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